Journal
ADVANCED SYNTHESIS & CATALYSIS
Volume 353, Issue 8, Pages 1325-1334Publisher
WILEY-BLACKWELL
DOI: 10.1002/adsc.201000917
Keywords
aqueous-phase catalysis; cyclodextrins; hydroformylation; hydrogenation; phosphane ligands
Categories
Funding
- Centre National de la Recherche Scientifique (CNRS)
- Ministere de l'Education et de la Recherche
- Reseau de Recherche
Ask authors/readers for more resources
A new triphenylphosphane based on a beta-cyclodextrin skeleton (PM-beta-CD-OTPP) was synthesized. This ligand can be dispersed in water by using the nanoprecipitation method. Transmission electron microscopy and NMR spectroscopy showed that PM-beta-CD-OTPP is aggregated in water and forms a stable dispersion. Its aqueous solubility can be dramatically increased in the presence of selected water-soluble guests by formation of inclusion complexes. Associated to a rhodium precursor, PM-beta-CD-OTPP is able to generate soluble rhodium species in water. In addition, NMR experiments showed that the cyclodextrin cavity remains accessible for a guest even when PM-beta-CD-OTPP is coordinated to rhodium. Finally, this ligand was efficient for rhodium-catalyzed hydrogenation and hydroformylation performed in aqueous medium.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available